EP3247306B1 - Interaktive führungs- und manipulationsdetektionsanordnungen für ein chirurgisches robotersystem - Google Patents

Interaktive führungs- und manipulationsdetektionsanordnungen für ein chirurgisches robotersystem Download PDF

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Publication number
EP3247306B1
EP3247306B1 EP16705612.6A EP16705612A EP3247306B1 EP 3247306 B1 EP3247306 B1 EP 3247306B1 EP 16705612 A EP16705612 A EP 16705612A EP 3247306 B1 EP3247306 B1 EP 3247306B1
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Prior art keywords
patient
interacting
user
instrument
interacting device
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EP16705612.6A
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English (en)
French (fr)
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EP3247306A1 (de
Inventor
Alon Mozes
Juan Salcedo
William Mcmahan
Ryan Anderson
Sarvagya VAISH
David Cole
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Neocis Inc
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Neocis Inc
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Priority to EP19214977.1A priority Critical patent/EP3653162B1/de
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Definitions

  • the present application relates to surgical robots and associated guidance systems and, more particularly, to a guided surgical robot system used, for example, in dental surgery, wherein the system is also configured to detect and be responsive to manipulation by / disengagement from a user thereof, as well as to interactively track the guided surgical instrument during the surgical procedure.
  • US 2014/0272789 A1 discloses a method of conducting a sinus lift procedure comprising forming a secure and physical interaction between a fiducial device and a site within a mouth of a patient to form a fiducial marker; forming a virtual incising plan for incising a portion of a maxilla of the patient; physically regulated movement of an incising device with respect to the fiducial marker; and providing tactile feedback to the user.
  • WO 2011/091382 A1 discloses a system comprising an attachment for fixing to a dental handpiece that comprises a handpiece drill, wherein the attachment comprises a sensor system that generates data usable to determine the position or angular orientation of the handpiece drill in relation to a reference surface engaged by the sensor system; a workpiece guide of a configuration of engage a dental arch of a patient, the workpiece guide including a known reference surface over an implant site and features for registering the sensor system to the workpiece guide; a computer system comprising a processor and a display; and an electronic interface that communicates the data from the sensor system to the computer system; wherein in use the sensor system is registered to the features of the workpiece guide and the sensor system engages the known reference surface of the workpiece guide, and the computer system receives the data from the sensor system, determines the position and angular orientation of the handpiece drill in relation to the patient's dentition based at least in part on the data from the sensor system, and displays, on a display, a display image that depict
  • a dental implant procedure generally involves several aspects: making the diagnosis, planning the position of the implant, surgically milling the anatomy and placing the implant (i.e., an anchoring post), and then attaching the abutment and crown (i.e., prosthetic tooth / teeth).
  • a procedure may be automated, for example, via a robotic surgical system.
  • Some surgical systems, such as dental implantation surgical systems may implement planning of the surgical procedure based on non-invasive imaging of the planned surgical site (i.e., via a CT scan).
  • the result of the plan namely the collected image(s) of the surgical site or patient anatomy, can thus be used, for example, for diagnosis, for manufacturing a drill guide, or for guiding haptic or autonomous robotic systems.
  • haptic robotic systems are configured to interact with the user/surgeon by responding to the forces applied by the user/surgeon during the procedure.
  • the surgical instrument i.e., drill
  • the surgical instrument may be generally arranged to be mounted on or in association with suitable force sensors.
  • "gravity compensation” may sometimes be required to counteract or compensate for the force of gravity on the arm(s) (i.e., in order to make the arm(s)/surgical instrument feel weightless to the user/surgeon).
  • a surgical robotic system and method having the capability of determining whether the user was actively engaging with the system, so as to better respond to the actual forces involved and acting upon the arm(s)/surgical instrument.
  • Such capabilities may also desirably facilitate safety of the system, for example, by having the capability of detecting movement of the arm(s)/surgical instrument in stances where the user is not actively engaged with or holding the surgical instrument.
  • some navigated and/or guided medical devices may provide feedback to the user, for example, via software-enabled visualizations, physical haptics, and/or audio cues, though such forms of feedback may not necessarily intuitive for the user.
  • some existing feedback methods may implement a "flight simulator" style of visual guide (see, e.g., FIG. 1 ) that may simultaneously display circles/crosshairs in relation to a target site on a number of two-dimensional images, which requires the user to manipulate the surgical instrument so as to line up the circles/crosshairs with the target on each image in the array of 2D images: Manipulating the surgical instrument in such an environment may not necessarily be intuitive to the user (surgeon), perhaps even with significant experience using the system.
  • a surgical robotic system and method having feedback capabilities that more intuitively guide the user in effectively and efficiently manipulating the surgical instrument during the surgical procedure.
  • Such capabilities may also desirably facilitate safety of the system, for example, by reducing "trial and error" manipulation of the surgical instrument by the user, particularly if the user is not significantly experienced with the system.
  • a dental implantation system in accordance with claim 1, comprising a patient-interacting device having an instrument adapted to at least interact with and prepare a site within a mouth of a patient for receiving a dental implant.
  • a guiding device is in communication with a fiducial marker adapted to be engaged with the mouth of the patient, wherein the guiding device is configured to receive the patient-interacting device.
  • the guiding device is also configured to guide the instrument of the patient-interacting device, relative to the fiducial marker, in conjunction with manipulation of the patient-interacting device by a user.
  • a controller device includes a processor, and is configured to be in communication with the guiding device.
  • the controller device is also configured to direct the patient-interacting device via the guiding device to prepare the site to receive the dental implant.
  • An engagement sensor is operably engaged with the patient-interacting device, and is configured to be in communication with the controller device. The engagement sensor is further responsive to disengagement between the patient-interacting device and the user to direct the guiding device to at least maintain the patient-interacting device at a minimum vertical disposition.
  • the disclosure includes a dental implantation method, comprising guiding an instrument of a patient-interacting device, via a guiding device and relative to a fiducial marker adapted to be engaged with a mouth of a patient, in conjunction with manipulation of the patient-interacting device by a user, wherein the patient-interacting device is received by the guiding device, and the instrument is configured to interact with and prepare the site within the mouth of the patient for receiving a dental implant.
  • the patient-interacting device is guided, via the guiding device, to prepare the site to receive the dental implant, via a controller device including a processor, wherein the controller device is configured to be in communication with the guiding device.
  • the guiding device is directed to at least maintain the patient-interacting device at a minimum vertical disposition, via the controller device, in response to disengagement between the patient-interacting device and the user, as determined by an engagement sensor operably engaged with the patient-interacting device and configured to be in communication with the controller device.
  • the disclosure further includes a dental implantation method, comprising guiding an instrument of a patient-interacting device, via a guiding device and relative to a fiducial marker adapted to be engaged with a mouth of a patient, in conjunction with manipulation of the patient-interacting device by a user, wherein the patient-interacting device is received by the guiding device, and the instrument is configured to interact with and prepare the site within the mouth of the patient for receiving a dental implant; displaying a real-time representation of the instrument of the patient-interacting device on a display device, in relation to a representation of the mouth of the patient, during manipulation of the patient-interacting device by the user; directing the patient-interacting device, via the guiding device and according to a dental implantation plan, to prepare the site to receive the dental implant, via a controller device including a processor, wherein the controller device is configured to be in communication with the guiding device and the display device; directing tactile feedback to the user, via the patient-interacting device, if the instrument manipulated by the user deviates from the virtual implantation plan
  • the disclosure further includes a dental implantation system, wherein such a system comprises a patient-interacting device having an instrument adapted to at least interact with and prepare a site within a mouth of a patient for receiving a dental implant; a guiding device in communication with a fiducial marker adapted to be engaged with the mouth of the patient, wherein the guiding device is configured to receive the patient-interacting device, and to guide the instrument of the patient-interacting device, relative to the fiducial marker, in conjunction with manipulation of the patient-interacting device by a user; a display device configured to display a real-time representation of the instrument of the patient-interacting device, in relation to a representation of the mouth of the patient, during manipulation of the patient-interacting device by the user; and a controller device including a processor, and configured to be in communication with the guiding device and the display device, wherein the controller device is configured to direct the patient-interacting device, via the guiding device and according to a virtual implantation plan, to prepare the site to receive the dental implant, and to direct tactile feedback to the user,
  • controller device is further configured to direct the display device to display an animation of the virtual representation of the instrument of the patient-interacting device manipulated in accordance with the virtual implantation plan, and wherein the animation originates from a disposition of the real-time representation of the instrument of the patient-interacting device.
  • controller device is further configured to direct the display device to display a progress indicia originating from the disposition of the real-time representation of the instrument of the patient-interacting device, and progressing in relation to a required manipulation of the patient-interacting device for the instrument to be in accordance with the virtual implantation plan.
  • the progress indicia comprises one of a distance originating from the disposition of the real-time representation of the instrument to a disposition of the instrument in accordance with the virtual implantation plan, and a degree of rotation originating from the disposition of the real-time representation of the instrument to a disposition of the instrument in accordance with the virtual implantation plan.
  • the audio device is configured to emit a selected audio signal, the selected audio signal increasing in frequency from the disposition of the real-time representation of the instrument toward a disposition of the instrument in accordance with the virtual implantation plan.
  • the guiding device is configured to provide a low resistance to manipulation of the patient-interacting device on one of manipulation of the patient-interacting device to move the instrument along a pathway in accordance with the virtual implantation plan, and manipulation of the patient-interacting device to rotate the instrument to a degree of rotation in accordance with the virtual implantation plan, and wherein the guiding device is further configured to provide a high resistance to manipulation of the patient-interacting device if one of the movement of the instrument along the pathway and rotation of the instrument deviates from the virtual implantation plan.
  • Various aspects of the present disclosure may be at least partially based on a guided surgical robotic system and method such as that disclosed, for example, in U.S. Patent No. 8,808,000 to Salcedo et al. and assigned to Neocis, also the assignee of the present application.
  • a dental implantation procedure generally involves an invasive incision into the gum of the patient in order to allow the practitioner to view the underlying jawbone structure. A hole is then drilled into the jawbone structure, into which a dental implant is placed (see, e.g., FIG. 2A ).
  • the dental implant may be shaped, for example, like a screw or other threaded member.
  • the practitioner may be able to graphically visualize the jawbone structure, without or before the invasive incision.
  • CT computerized tomography
  • the alignment of the dental implant with respect to the jawbone structure and/or relative to other implants or teeth may be an important factor in determining, for example, the life of the dental implant, the appearance thereof, and the comfort to the patient. If the dental implant is poorly or otherwise not optimally placed, the dental implant can undesirably fail (or at least have a shorter service life), may undesirably cause other teeth or dental implants to be compromised, and/or damage proximal nerves.
  • FIGS. 3 and 4 thus illustrate various aspects of a dental implantation system according to the present disclosure, the system being generally indicated by the numeral 100.
  • current dental implantation procedures generally involve an imaging step, wherein CT or other appropriate images of the patient's jaw structure are obtained, and any anomalies diagnosed (i.e., whether the patient requires bone grafts to prepare the implant area). The practitioner then corrects any anomalies and proceeds with the invasive implant procedure based on the conditions associated with the patient's jaw structure, once the appropriate incisions have been made in the patient's gum.
  • the various systems and method disclosed herein may be readily applicable, or otherwise readily adaptable, to other surgical procedures that are proximal to or otherwise capable of being correlated with the fiducial marker associated with the engagement between a splint or other engaging member, and the jaw structure of the patient, as otherwise disclosed herein (i.e., brain surgery, skull surgery, ENT surgery, or any other surgical procedure associated with the head/skull structure of the patient).
  • a dental implantation system 100 addresses particular subjective aspects of current dental implantation procedures by providing a guided patient-interacting device 150 (otherwise referred to herein as a "cutting device” or “drilling device” or “site preparation device” or “implantation device” depending on the particular instrument 500 engaged with the patient-interacting device 150 so as to configure the patient-interacting device 150 for a particular corresponding purpose or procedure) configured to be guided with respect to the invasive portion, or at least the patient-interacting portion, of the dental implant procedure (i.e., to "prepare” the site within or otherwise engage the patient's mouth).
  • a guided patient-interacting device 150 otherwise referred to herein as a "cutting device” or “drilling device” or “site preparation device” or “implantation device” depending on the particular instrument 500 engaged with the patient-interacting device 150 so as to configure the patient-interacting device 150 for a particular corresponding purpose or procedure
  • the patient-interacting device 150 is operably engaged with a guiding device 200, such as, for example, an articulating arm member 350 (i.e., a robotic arm).
  • the guiding device 200 is adapted to operably engage or otherwise be in communication with the mouth of the patient, for example, by way of a splint 250 or other engaging member, forming or otherwise defining a fiducial marker. That is, in one instance, the splint 250 is configured to engage the patient's mouth in a "firm" or secure interaction (i.e., the splint 250 is engaged with the patient's teeth and does not move with respect to the patient's mouth).
  • the disposition of the splint 250 is known, and thus can be configured to provide a fiducial marker (i.e., a known origin or coordinate formed by the secure interaction with or otherwise associated with or attached to the splint 250) which can be used, for instance, to guide the patient-interacting device / instrument, via the guiding device 200, to prepare the site in the patient's mouth in association with the dental implant 300 (see, e.g., FIG. 2B ).
  • a fiducial marker i.e., a known origin or coordinate formed by the secure interaction with or otherwise associated with or attached to the splint 250
  • the splint 250 is configured to be "universally applicable” (i.e., capable of forming the secure engagement with the mouth of any patient), or at least applicable across a particular range of patients (i.e., one size fits a certain size or age of patient).
  • the splint 250 may be engaged with the patient's teeth, and the patient's jawbone structure then imaged using, for example, CT or any other suitable imaging technique such as, for instance, MRI.
  • the fiducial marker can thus be established, for instance, as a reference origin of a relative coordinate system.
  • the splint 250 may be configured in many different manners to accomplish the desired function as discussed herein.
  • the splint 250 may be rigidly attached to the patient's mouth in an appropriate manner depending on the condition of the patient. That is, if the patient has some strong teeth capable of supporting the splint 250, the splint 250 can be attached to the teeth with an adhesive or with a suitable clamp.
  • bone pins may be drilled through the splint 250 and into the patient's jawbone structure to fasten the splint 250 securely into place.
  • the splint 250 may also be attached to the jawbone structure of any patient using, for example, appropriate bone screws.
  • the positioning of the splint 250 with respect to the patient's mouth may not be critical or important, as long as the splint 250 remains rigidly in place.
  • a fiducial marker (not shown) may then be formed by the secure engagement, or may otherwise be attached to, or incorporated into, or associated with the splint 250, wherein the fiducial marker may be configured to have a geometry or other characteristic or feature that uniquely defines the fiducial marker in a three-dimensional space (i.e., such that the fiducial marker is readily identified in images of the patient's jawbone structure, or is otherwise detectable and trackable using a mechanical arrangement, an electrical arrangement, an electromechanical arrangement, an optical arrangement, a magnetic arrangement, or any other suitable detection/tracking arrangement, or combination thereof).
  • the fiducial marker may be comprised of, for example, a radiopaque material that can be clearly defined in the image obtained, e.g., by CT or MRI.
  • the patient-interacting device 150 may be engaged with the guiding device 200, for example, in the form of an articulating arm member or a robotic arm 350, which is configured to determine a range of motion of the patient-interacting device 150/instrument 500 (i.e., translation in a particular direction (horizontal and/or vertical), and/or rotation about an axis).
  • the functionality of the guiding device 200 may be included in the configuration and arrangement of the articulating arm member 350, itself.
  • the articulating arm member 350 or portions thereof may include or be engaged with one or more actuators configured and arranged to cooperate to guide a distal end of the articulating arm member 350 in a desired direction and orientation, upon manipulation by the user to accomplish the surgical procedure.
  • the guiding device 200 may further comprise a communication element 400 in communication between the splint 250 and the patient-interacting device 150 and/or between the splint 250 and the arm member 350.
  • the communication element 400 may comprise a mechanical linkage connecting the splint 250 to the patient-interacting device 150 or to the arm member 350. That is, the communication element 400 may comprise, for example, a mechanically- or physically-tracked arm which attaches to the splint 250 engaged with the patient.
  • the arm (communication element 400) may be attached to the splint 250 (rigidly and in a known, repeatable manner) with an attachment mechanism comprising a kinematic mount (i.e., a kinematic mount may be engaged between the arm and the splint 250).
  • an attachment mechanism comprising a kinematic mount (i.e., a kinematic mount may be engaged between the arm and the splint 250).
  • the communication element 400 may be tracked or otherwise monitored to provide data (whether constantly, selectively, or otherwise as necessary) about the position of the patient (i.e., with respect to the fiduciary or fiducial marker) to the patient-interacting device 150 and/or to the arm member 350, while still providing for accurate guidance of the patient-interacting device 150 and/or the arm member 350, in the event that the patient moves during the surgical procedure.
  • the splint 250 and/or the fiducial marker determined thereby may be communicated to the patient-interacting device 150 and/or to the arm member 350 in many different manners.
  • the fiducial marker may be communicated via a communication element 400 comprising a wireless transceiver, a hardwire connection, an optical communication system (i.e., a camera or other video device), an acoustic tracking system, or any other suitable mechanism, whether electrical, mechanical, electromechanical, acoustic, or optical in nature.
  • the kinematic mount itself, may comprise an attachment point for a tracking portion (and/or the tracking arm or other tracking provision) associated with the guidance system for the surgical robot (i.e., wherein, for instance, reflective markers may be mounted to the attachment point for optical tracking of the fiducial marker or the splint device itself, or the attachment point may include a securing site for forming a mechanical connection therewith for mechanical tracking of the fiducial marker, or the attachment point may otherwise be configured to receive an appropriate element associated with any other suitable tracking arrangement for the fiducial marker, whether electrical, mechanical, electromechanical, acoustic, or optical in nature).
  • the kinematic mount may be configured or otherwise arranged to function as a fixed mounting site for particular tracking devices such as, for example, one or more markers that may be permanently affixed to the kinematic mount 500 and configured to be trackable by an optical-type tracking device (i.e., an optical tracking marker).
  • tracking devices such as, for example, one or more markers that may be permanently affixed to the kinematic mount 500 and configured to be trackable by an optical-type tracking device (i.e., an optical tracking marker).
  • the system 100 may be further configured to include a controller device 450 (i.e., a computer device as shown in FIG. 4 ) for determining, controlling, or tracking the fiducial marker with respect to the image of the patient's mouth having the splint 250 disposed therein.
  • the controller device 450 may also be configured and arranged to appropriately communicate the fiducial marker to the patient-interacting device 150 and/or to the arm member 350.
  • the system 100 or the controller device 450 may also comprise a planning device or otherwise include planning functionality for allowing a user to develop the virtual implantation plan, as otherwise disclosed herein, in conjunction with the hardware and/or software of the system 100.
  • the controller device 450 may be further configured to receive the image of the patient's jawbone structure (having the splint 250 therein).
  • the controller device 450 which includes a processor, may be further configured to be capable of executing a planning routine that may comprise software, hardware, or a combination thereof (i.e., a planning device and/or planning functionality).
  • the planning routine thus allows the practitioner to create, for example, a virtual implantation plan based on the captured image(s), whether in two dimensions or three dimensions, and to manipulate the image(s) of the patient's jawbone structure in conjunction with a "virtual implant” in order to develop the virtual implantation plan or placement determination of the prosthesis for the patient, in conjunction with a computerized model based on the image(s).
  • the planning routine, virtual implantation plan, and/or placement determination may be created in relation, for example, to a coordinate system (relative or absolute), as will be appreciated by one skilled in the art, configured to associate the planning parameters with the fiducial marker.
  • the controller device 450 and/or the planning device associated therewith may include a peripheral device (i.e., a trackball or joystick in conjunction with, for example, 3D goggles, all not shown) to assist with or otherwise permit virtual manipulation of the placement of the virtual implant(s) with respect to the image(s) of the patient's jaw structure in order to, for example, align the implant(s) relative to each other or relative to adjacent teeth, to align the implant(s) relative to the affected nerve, and/or to align the implant(s) relative to the jawbone structure.
  • the controller device 450 and/or the planning device may be further configured to perform such manipulation manually, automatically, or semi-automatically, as necessary or desired.
  • the orientation or placement of the virtual implant(s) may represent the desired actual placement of the implant with respect to the patient's jawbone structure, thus providing an intuitive interface for planning the implantation procedure.
  • the patient is automatically registered with the system 100 / controller device 450 once the communication element 400 is attached to or otherwise engaged or in communication with the splint 250 via the kinematic mount of the attachment mechanism. That is, the fiducial marker is automatically determined from the image(s) of the patient's jawbone structure, and the alignment and location thereof in physical space is known due to the kinematic mount connecting the communication element 400 (i.e., arm) to the splint 250.
  • a surface matching technique can be implemented.
  • the patient's jawbone structure may be manipulated into a 3D configuration in the captured image(s).
  • a suitable scanning device i.e., a physical pointer or other imaging device such as an ultrasound transducer or OCT (optical coherence tomography) scanner may be attached to an end effector (i.e., tip) of the arm member 350 such that the tip of the arm member 350 is capable of scanning the patient's jawbone structure to "surface match" the captured and manipulated image(s) with an actual scan of the jawbone structure, as administered, for example, via the controller device 450.
  • OCT optical coherence tomography
  • association of the fiducial marker with the patient's anatomy, via the controller device 450 may be accomplished in different manners.
  • the registration of the image (e.g., CT scan) to the fiducial marker one method could involve the jaw structure of the patient being imaged with the fiducial marker in place, as previously discussed, wherein the patient would then be substantially immediately subjected to the implantation procedure.
  • Such a scheme may be beneficial, for example, in reducing the number of visits to the practitioner by the patient.
  • the practitioner may not have the imaging capabilities at hand, or may prefer to carefully determine the virtual implantation plan before carrying out the implantation procedure.
  • a pre-operative imaging procedure (e.g., CT scan) may be performed on the jaw structure of the patient, without a fiducial marker in place (i.e., a "normal" scan by which the practitioner can determine the virtual implantation plan).
  • This pre-operative imaging procedure can thus be performed, for example, at the practitioner's site, or at a dedicated scanning/imaging center.
  • the practitioner may capture another image (e.g., CT scan, panoramic x-ray, or two single x-rays) of the patient's jaw structure.
  • the controller device 450 / planning device may thus also be configured to correlate the pre-operative image (used to determine the virtual implantation procedure) with the "day of" image so as to register the fiducial marker(s) with respect to the original pre-operative image.
  • Such a registration or correlation procedure may be implemented in hardware, software, or a combination thereof, as will be appreciated by one skilled in the art.
  • the implantation procedure could then proceed as otherwise disclosed herein.
  • the communication element 400 may be configured to communicate with the arm member 350 in a manner known to the system 100, such that the position/movement characteristics of the end effector /tip thereof are also known.
  • This engagement between the communication element 400 and the arm member 350 thus allows the patient-interacting device 150/instrument 500 (i.e., the end effector / tip) to be registered with respect to the fiducial marker (or other reference with respect to the patient) attached to the patient via the splint 250, the kinematic mount, the communication element 400, and the arm member 350.
  • the virtual implantation process, planned through the controller device 450 / planning device may be accomplished in relation to the fiducial marker (or other reference with respect to the patient) and thus translated or otherwise communicated to the system 100 for directing the patient-interacting device 150/instrument 500 via the guiding device 200 and the arm member 350.
  • the communication element 400 may, in some instances, be configured to communicate between the splint 250 / kinematic mount and the controller device 450 / planning device (and/or between the splint 250 / kinematic mount and the patient-interacting device 150/instrument 500), based upon the premise of establishing a known association of the fiducial marker with the patient's anatomy, in relation to which the guiding device 200 is used to guide the patient-interacting device 150/instrument 500 via the arm member 350 during the implantation procedure.
  • the patient-interacting device 150/instrument 500 may comprise, be disposed in, or otherwise engaged with the end effector of the arm member 350 (robotic arm).
  • the arm member 350 may be configured, for example, to provide six degrees of freedom and can also be configured to restrict or otherwise control the movement of the patient-interacting device 150/instrument 500.
  • the arm member 350 may have a miniature parallel structure to which the patient-interacting device 150 is secured and allowed to have full freedom of movement when not in cutting/preparation/implantation mode. Since the patient-interacting device 150/instrument 500 comprises or is attached to the end effector of the arm member 350, the patient interacting portion (i.e., the cutting/drilling tip) is the instrument 500 (see, e.g., FIG.
  • a calibration element may be engaged with the patient-interacting device 150 via a kinematic coupling (i.e., rigidly mounted thereto in a known, repeatable manner).
  • a kinematic coupling i.e., rigidly mounted thereto in a known, repeatable manner.
  • the calibration element is replaced with a cutting/drilling element (instrument 500) in the patient-interacting device 150, in a known and repeatable manner, so that the calibration parameters (i.e., the position of the distal-most point and axis of cutting/drilling) associated with the interacting portion/instrument 500 are maintained as calibrated.
  • the implantation procedure i.e., cutting/drilling/insertion
  • the practitioner moving the patient-interacting device 150/instrument 500 toward the patient's mouth (having the splint 250 engaged therewith).
  • the controller device 450 / planning device is configured to control, restrict, or otherwise modulate the movement of (or the practitioner's ability to move) the patient-interacting device 150 via the arm member 350 such that the action of the practitioner merely moves the interacting portion/instrument 500 (i.e., the cutting/drilling element) to the appropriate starting position for the implantation procedure, with respect to the patient's jawbone structure, as determined by the controller device 450 / planning device and dictated by the virtual implantation plan.
  • the controller device 450 / planning device may further dictate other parameters of the implantation device 150/instrument 500 such as, for example, the orientation of the path of the cutting/drilling element (instrument 500) and the cutting/drilling distance along that path from the cutting/drilling origin, also according to the virtual implantation plan.
  • the system 100 disclosed herein may be configured such that the patient-interacting device 150 is not guided by the practitioner, but is only urged by the practitioner along a procedural route determined via the virtual implantation plan and implemented via the controller device 450 / planning device and the arm member 350.
  • the system 100 may be configured to restrict the practitioner to performing the implantation procedure with respect to the patient, as determined via the virtual implantation plan and implemented via the controller device 450 / planning device and the arm member 350, whereby the controller device 450 / planning device controls the allowable movement of the arm member 350 (and thus the patient-interacting device 150/instrument 500) in accordance with the virtual implantation plan created from the image(s) of the patient's jawbone structure.
  • the system 100 may be configured for restricted movement of the arm member 350/ patient-interacting device 150/instrument 500, as communicated to the practitioner through tactile/haptic feedback, where, for example, the arm member 350 / patient-interacting device 150 / instrument 500 may be easier to move according to the virtual implantation plan, and more difficult to move if deviating from the virtual implantation plan.
  • the physical structure of the arm member 350 / patient-interacting device 150 / instrument 500 may not necessarily be configured to provide full and absolute controlled movement according to the virtual implantation plan (i.e., due to vibration, flexing of components, gravity, and/or excessive force applied by the practitioner) and, as such, the system 100 / controller device 450 may be further configured to provide other manners of feedback to the practitioner such as, for example, via a deviation warning indicia, haptic feedback, or any other suitable audio and/or visual and/or any other suitable mechanism.
  • the system 100 / controller device 450 includes provisions for actually implementing the virtual implantation plan, and thus facilitates a more accurate implantation procedure, rather than merely warning the practitioner if any procedural parameters may be inaccurate.
  • the system 100 may be further configured to autonomously accomplish the virtual implantation plan, without the manipulation of the practitioner, through automatic manipulation of the arm member 350 / patient-interacting device 150 / instrument 500 via the controller device 450 / planning device.
  • the splint 250 i.e., mouthpiece
  • the splint 250 is first attached to the patient's teeth, and thus provides or is associated with a fiducial marker.
  • the patient's jawbone structure is then imaged (with the splint 250 in place and engaged with the patient's teeth) using, for example, CT or any other appropriate imaging technique (e.g., MRI), and the image(s) communicated to the controller device 450.
  • the controller device 450 may be further configured to be capable of executing an implantation routine, thus allowing the practitioner to develop an implantation plan for the patient, for example, by manipulating a virtual implant with respect to the captured image(s).
  • the communication element 400 is engaged with (i.e., attached to the patient's mouth, with the patient being positioned in a suitable position to initiate the procedure) or otherwise placed into communication with the splint 250 (i.e., via the kinematic mount).
  • the arm member 350, patient-interacting device 150, and interacting portion / instrument 500 thereof, are then calibrated by the practitioner (or automatically by the controller device 450), before the actual cutting/drilling element (instrument 500) of the patient-interacting device 150 is used by the practitioner (or autonomously via the controller device 450 / planning device), via the patient-interacting device 150 as guided by the arm member 350 and the controller device 450, to accomplish the implantation procedure as planned and dictated by the virtual implantation plan.
  • haptic or feedback-based robotic systems may be configured to interact with the user/surgeon by responding to the forces applied by the user/surgeon during the procedure.
  • the surgical instrument i.e., drill
  • the surgical instrument may be generally arranged to be mounted on or in association with suitable force sensors.
  • "gravity compensation” may sometimes be required to counteract or compensate for the force of gravity on the arm(s) (i.e., in order to make the arm(s)/surgical instrument feel weightless to the user/surgeon).
  • aspects of the present disclosure may provide a dental implantation system 100, as previously disclosed, wherein the patient-interacting device 150 / instrument 500 is adapted to at least interact with and prepare a site within a mouth of a patient for receiving a dental implant, and the guiding device 200 in communication with the fiducial marker is configured to receive the patient-interacting device 150, and to guide the instrument 500 relative to the fiducial marker, in conjunction with manipulation of the patient-interacting device 150 by the user.
  • the controller device 450 including a processor, is configured to be in communication with the guiding device 200, and to direct the patient-interacting device 150 via the guiding device 200 to prepare the site to receive the dental implant.
  • an engagement sensor 750 is operably engaged with the patient-interacting device 150 (see, e.g., FIG. 5 ), wherein the engagement sensor 750 is configured to be in communication with the controller device 450.
  • the engagement sensor 750 is further configured to be responsive to disengagement between the patient-interacting device 150 and the user, so as to direct the guiding device 200 to at least maintain the patient-interacting device 150 at a minimum vertical disposition.
  • the system may sometimes have difficulty discerning between the various forces involved and acting upon the arm member 350 / patient-interacting device 150 such as, for example force applied by the user, any drift of the force sensor which may result in the detection of "phantom” forces, the force of gravity, or the force of resistance (i.e., from the drill drilling into the patient's bone structure), etc.
  • the counteracting or compensating force provided by the controller 450 i.e., by way of the arm member 350
  • the engagement sensor 750 is arranged with respect to the patient-interacting device 150 so as to determine when the user is actively engaged or disengaged from the patient-interacting device 150 (i.e., whether the user is gripping the patient-interacting device 150 or not).
  • the controller device 450 may be able to eliminate any effects of drift on the patient-interacting device 150 by the guiding device 200 (i.e., since the engagement sensor 750 is not actuated, the controller device 450 knows that any indicated forces on the guiding device 200 / patient-interacting device 150 are not originating from use interaction with the patient-interacting device 150).
  • the determination of disengagement between the patient-interacting device 150 and the user by the engagement sensor 750 may cause the controller device 450 to direct the guiding device 200 to at least maintain the patient-interacting device 150 at a minimum vertical disposition (i.e., the patient-interacting device 150 / arm member 350 is prevented from falling or downwardly creeping due to gravity), upon release of the patient-interacting device 150 by the user. Thereafter, any movement of the guiding device 200, arm member 350, and/or the surgical instrument (i.e., the patient-interacting device 150 / instrument 500), in instances where the user is not actively engaged with or holding the surgical instrument, may be readily detected by the controller device 450 and the disengaged position of the patient-interacting device 150 to be determined.
  • a minimum vertical disposition i.e., the patient-interacting device 150 / arm member 350 is prevented from falling or downwardly creeping due to gravity
  • At least one force sensor may be operably engaged with, for example, the guiding device 200 and/or the patient-interacting device 150, wherein the at least one force sensor may be configured to measure a force or forces acting on the patient-interacting device 150, and to communicate the measured force to the controller device 450.
  • the controller device 450 may be responsive to the determination of disengagement from the engagement sensor 750 by the user to zero the measured force from the at least one force sensor (i.e., such that any indicated forces later appearing on the guiding device 200 / patient-interacting device 150 are ascertained to not be originating from use interaction with the patient-interacting device 150).
  • the engagement sensor 750 may be further configured to be responsive to disengagement between the patient-interacting device 150 and the user to direct the guiding device 200 (i.e., via the controller device 450) to maintain the patient-interacting device 150 at a selected lateral disposition and/or a selected rotational orientation. That is, in addition to or in the alternative to maintaining the patient interacting device 150 at a minimum vertical disposition, the patient-interacting device 150 may also be restricted from moving laterally or sideways, or rotating about the longitudinal axis thereof, by the controller 450 / guiding device 200, if the engagement sensor 750 does not detect engagement between the user and the patient-interacting device 150.
  • the engagement sensor 750 may be configured to be responsive to engagement between the patient-interacting device 150 and the user to actuate the guiding device 200, for example, by way of the controller device 450, to guide at least the instrument 500 of the patient-interacting device 150, relative to the fiducial marker, and/or to direct the controller device 450 to actuate the virtual implantation plan for guiding at least the instrument 500 of the patient-interacting device 150. Additionally, the engagement sensor 750 may be configured to be responsive to engagement between the patient-interacting device 150 and the user to at least permit the instrument 500 to be actuated.
  • the engagement sensor 750 may require the detection of engagement between the patient-interacting device 150 and the user in order for the patient-interacting device 150 / instrument 500 to be actuatable or otherwise operable to carry out the surgical procedure.
  • the user may be required to engage the patient-interacting device 150, as detected by the engagement sensor 750, in order to allow the virtual implantation plan to be actuated and/or for the guiding device 200 to provide the appropriate guidance for the user-manipulated patient-interacting device 150.
  • the system 100 may be configured such that the controller device 450 is configured to execute the virtual implantation plan for the site within the mouth of the patient, and to direct the guiding device 200 according to the virtual implantation plan, in response to engagement of the engagement sensor 750 by the user.
  • the controller device 450 may be configured to direct tactile feedback to the user, via the patient-interacting device 150 (i.e., tactile or haptic feedback via the patient-interacting device to the hand of the user grasping the patient-interacting device 150 and engaging the engagement sensor 750), if the instrument 500 manipulated by the user deviates from the virtual implantation plan. Further, the controller device 450 may be configured to direct at least one of audio feedback and visual feedback to the user, via at least one of the controller device 450 and the patient-interacting device 150, if the instrument 500 manipulated by the user deviates from the virtual implantation plan.
  • the system 100 may further comprise a display device 800 (see, e.g., FIGS. 4 and 5 ) in communication with the controller device 450 and/or the patient-interacting device 150.
  • the display device 800 may be configured to display a real-time representation of at least the instrument 500 of the patient-interacting device 150, in relation to a representation of the mouth of the patient, during engagement with and manipulation of the patient-interacting device 150 by the user.
  • the controller device 450 may also be configured to be in communication with the guidance device 200 and the display device 150, wherein the controller device 450 may be configured to monitor manipulation of at least the instrument 500 of the patient-interacting device 150 by the user, in relation to the mouth of the patient, at least partially via the guidance device 200, and to direct information associated therewith to the display device 800.
  • the engagement sensor 750 may be implemented in many different manners, as will be appreciated by one skilled in the art.
  • the engagement sensor 750 may be operably engaged with the patient-interacting device 150, and may comprise, for example, one of a touch-sensitive actuator, a pressure-sensitive actuator, an optical actuator, and an acoustic actuator, associated with the patient-interacting device 150.
  • detection of the user's grip on the patient-interacting device 150 may be implemented by way of, for example, an engagement sensor 750 comprising a camera, an infrared sensor, an acoustic sensor, a range-finder, or other appropriate sensor that is engaged with or in proximity to the patient-interacting device 150 to determine if actual contact is made with the patient-interacting device 150, or if an object that can be identified, for example, as a hand of the user, intercedes between the sensor and the patient-interacting device 150.
  • an engagement sensor 750 comprising a camera, an infrared sensor, an acoustic sensor, a range-finder, or other appropriate sensor that is engaged with or in proximity to the patient-interacting device 150 to determine if actual contact is made with the patient-interacting device 150, or if an object that can be identified, for example, as a hand of the user, intercedes between the sensor and the patient-interacting device 150.
  • the engagement sensor 750 may comprise, for example, an appropriate pressure switch or sensor mounted on the patient-interacting device 150, a sleeve placed over the patient-interacting device 150 which, in cooperation, can indicate physical contact by closing an electrical contact or sensing pressure in response to the grip of the user's hand.
  • the engagement sensor 750 may also be configured to measure or otherwise determine the magnitude of the force exerted via the user's grip on the patient-interacting device 150, wherein the measured force magnitude could be directed to the controller device 450 or elsewhere in the system 100 as necessary or appropriate.
  • the engagement sensor 750 (as well as other components such as, for example, the fiducial marker), may be established in communication with the controller device 450 and/or other components in the system 100, for example, by way of an electrical communication system, a mechanical communication system, an electromechanical communication system, an optical communication system, and combinations thereof, or through any other suitable communication arrangement, as will be appreciated by one skilled in the art, wherein the communication system or communication arrangement may, for example, comprise a wireless communication system and/or a wired communication system.
  • the planning of or actually conducting the surgical procedure by way of, for instance, the controller device 450 and/or the planning device and/or planning functionality associated therewith may be enhanced by incorporating real-time intuitive feedback into the virtual implantation plan (i.e., as opposed to the virtual implantation plan being created solely based upon the imaging of the patient's mouth and used as a reference by the surgeon).
  • a drill, probe, or other instrument 500 engaged with or forming the patient-interacting device 150 may be manipulated by the user (i.e., surgeon) in relation to the site within the patient's mouth.
  • the manipulation of the patient-interacting device 150 /instrument 500 by the user can be monitored in real-time by the controller device 450 / planning device, in relation to the actual anatomy associated with the site within the patient's mouth or in relation to a model thereof.
  • the system 100 may also include a display device 800 (see, e.g., FIGS. 4 and 5 ) in communication with the controller device 450 / planning device, and configured to receive and display a real-time representation of the patient-interacting device 150 /instrument 500 in relation to a representation of the mouth of the patient (i.e., the actual anatomy imaged during the manipulation or a model or other representation thereof otherwise determined) during manipulation of the patient-interacting device 150, such that the user can see or visualize feedback of the manipulation of the patient-interacting device 150 / instrument 500 on the display device 800 in real time.
  • a display device 800 see, e.g., FIGS. 4 and 5
  • a display device 800 in communication with the controller device 450 / planning device, and configured to receive and display a real-time representation of the patient-interacting device 150 /instrument 500 in relation to a representation of the mouth of the patient (i.e., the actual anatomy imaged during the manipulation or a model or other representation thereof otherwise determined) during manipulation of the patient-interacting device 150,
  • the dental implant position, the site within the patient's mouth, and/or the surgical (dental implantation) plan could be projected in a virtual manner on the display device 800, such that the user could visualize a simulation of the surgical procedure in relation to the physical manipulation of the patient-interacting device 150 /instrument 500 by the user, and in real time.
  • an implantation device 150 having a prosthetic member attached thereto may be moved or manipulated in relation to the site in the patient's mouth, and the user may concurrently view a representation of the implantation device 150 having the virtual dental implant engaged therewith on the display device 800, in relation to a virtual projection of the interaction of the dental implant with the site within the patient's mouth, while the manipulation is occurring.
  • the controller device 450 / planning device may be configured to relate the manipulation of the patient-interacting device 150 / instrument 500 by the user to a previously-developed virtual implantation plan (or even initiate a virtual implantation plan based upon the manipulation), such that the virtual implantation plan can be updated and/or modified in relation to the manipulation by the user.
  • the virtual implantation plan can finalized or "locked in” by the user (i.e., the user can selectively indicate that the updates/modifications to the virtual implantation plan resulting from the manipulation are satisfactory, and the previously-existing virtual implantation plan can thus be updated/amended to include the same).
  • the finalized virtual implantation plan may be executed by the controller device 450 / planning device, with the system 100 being configured to be responsive to the executed virtual implantation plan to direct the manually-guided patient-interacting device (i.e., using haptic or tactile feedback to the user) or to direct an autonomous robotic system.
  • aspects of the present disclosure may also provide a dental implantation system 100, as previously disclosed, wherein the display device 800 (see, e.g., FIG. 6 ) is configured to display a real-time representation of the instrument 500 of the patient-interacting device 150 (see, e.g., FIG. 7 ), in relation to a representation of the mouth of the patient, during manipulation of the patient-interacting device 150 by the user.
  • the display device 800 see, e.g., FIG. 6
  • FIG. 7 a real-time representation of the instrument 500 of the patient-interacting device 150
  • the controller device 450 may further be configured to 1) direct the display device 800 to display the real-time representation 600 of the instrument 500 in relation to a virtual representation 650 of the instrument 500 of the patient-interacting device 150 manipulated in accordance with the virtual implantation plan; 2) direct an audio device 700 (see, e.g., FIG. 5 ) in communication with the controller device 450 to emit a selected audio signal indicative of the patient-interacting device 150 manipulated in accordance with the virtual implantation plan; and/or 3) direct the guiding device 200 to provide a selected resistance to manipulation of the patient-interacting device 150 in accordance with the virtual implantation plan.
  • the controller device 450 may be further configured to direct the display device 800 to display an animation of the virtual representation 650 of the instrument 500 of the patient-interacting device 150 manipulated in accordance with the virtual implantation plan, wherein the animation may originate from a current disposition of the real-time representation 600 of the instrument 500 of the patient-interacting device 150 also displayed by the display device 800. That is, the animation of the virtual representation 650 of the instrument 500 may indicate, via the animation, the direction (i.e., horizontal and/or vertical) in which the user must direct the patient-interacting device 150 and/or the direction of rotation in which the user must rotate the patient-interacting device 150 (see, e.g., FIG. 7 ), starting from the current disposition of the real-time representation 600 of the instrument 500, in order to move or manipulate the instrument 500 according to the virtual implantation plan.
  • the animation of the virtual representation 650 of the instrument 500 may indicate, via the animation, the direction (i.e., horizontal and/or vertical) in which the user must direct the patient-interacting device 150 and/or the direction of rotation
  • the controller device 450 may be further configured to direct the display device 800 to display a progress indicia 675, originating from the disposition of the real-time representation of the instrument 500 of the patient-interacting device 150, and progressing in relation to a required manipulation of the patient-interacting device 150 for the instrument 500 to be in accordance with the virtual implantation plan. That is, for example, in addition to the animation, the display device 800 may also display some indication of the progress of the user in moving the patient-interacting device 150 toward the site of the procedure.
  • Such an indication could be a progress bar graph indicating the distance or rotation that must occur from the current real-time representation of the instrument 500 to the surgical site, or the distance or rotation that must still occur before the instrument 500 is properly manipulated at the surgical site according to the virtual implantation plan. That is, the progress indicia 675 may comprise one of a distance originating from the disposition of the real-time representation of the instrument to a disposition of the instrument in accordance with the virtual implantation plan, and a degree of rotation originating from the disposition of the real-time representation of the instrument to a disposition of the instrument in accordance with the virtual implantation plan.
  • the audio device 700 may be configured, for example, to emit a selected audio signal, wherein the selected audio signal may increase or otherwise change in frequency from the disposition of the real-time representation of the instrument toward a disposition of the instrument in accordance with the virtual implantation plan.
  • the guiding device 200 may be configured to provide a low resistance to manipulation of the patient-interacting device 150, for instance, when the patient-interacting device 150 is manipulated by the user to move the instrument 500 along a pathway in accordance with the virtual implantation plan, and/or the patient-interacting device 150 is manipulated by the user to rotate the instrument 500 to a degree of rotation in accordance with the virtual implantation plan.
  • the guiding device 200 may be further configured to provide a high resistance to manipulation of the patient-interacting device 150 by the user, for example, if the movement of the instrument 500 along the pathway and/or the rotation of the instrument 500 deviates from the virtual implantation plan.
  • the guiding device 200 may be configured such that relatively less force is required from the user to move the patient-interacting device 150 according to the virtual implantation plan, while there may be significant resistance from the guiding device 200 if the user attempts to move the patient-interacting device 150 in deviation from the virtual implantation plan.
  • various combinations of feedback measures may be implemented by the system 100 that may help to make the user's manipulation of the patient-interacting device 150 according to the virtual implantation plan more intuitive.
  • visual feedback using a "ghost” tool i.e., a "ghost” instrument of a distinct color may be animated on the display device toward the destination of the surgical site, from the current instrument position.
  • the "ghost” tool may, in some instances, be provided in three-dimensions, with the 3D view may serve to clarify and make more intuitive to the user the direction in which the actual tool must be manipulated according to the virtual implantation plan.
  • a progress bar indicating "distance to goal” (in degrees for rotation or in a linear measurement for translation), may be provided.
  • the animation and the progress bar may be updated dynamically as the patient-interacting device 150 is manipulated by the user.
  • audio feedback may be used, for example, in the form of a dynamic beeping frequency, to indicate how close the patient-interacting device 150 is to the planned surgical site.
  • a lower frequency (i.e., slower) beeping may be audible when the patient-interacting device 150 is relatively far from the intended surgical site, while the frequency of the beeping may increase (i.e., faster) as the patient-interacting device 150 approaches the surgical site.
  • physical (haptic or tactile) feedback may be implemented, for example, to limit or restrict the motion of the guiding device 200 (i.e., arm member 350) so the user is strictly allowed to guide the patient-interacting device 150 along a particular path (in translation and / or rotation).
  • directional damping may also be provided via the guding device 200 / arm member 350, for example, to provide cues to the user that the patient-interacting device 150 is being moved the correct manner according to the virtual implantation plan.
  • the guiding device 200 / arm member 350 may be configured to provide relatively less resistance to movement of the patient-interacting device 150 along a "proper direction" according to the virtual implantation plan, and/or may be configured to provide relatively more or otherwise significant resistance to movement of the patient-interacting device 150 in the "wrong direction" deviating from the virtual implantation plan.
  • This relatively more resistance is not necessarily absolute resistance, but may allow, for example, the user to move the patient-interacting device 150 backwards in relation to the virtual implantation plan.
  • Such an aspect may be useful, for example, for translation of the patient-interacting device 150 / instrument 500 in small spaces and/or rotation of the patient-interacting device 150 / instrument 500 where the goal orientation is not necessarily easy to discern.
  • first, second, etc. may be used herein to describe various steps or calculations, these steps or calculations should not be limited by these terms. These terms are only used to distinguish one operation or calculation from another. For example, a first calculation may be termed a second calculation, and, similarly, a second step may be termed a first step, without departing from the scope of this disclosure.
  • the term "and/or" and the "/" symbol includes any and all combinations of one or more of the associated listed items.

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  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Surgery (AREA)
  • Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Medical Informatics (AREA)
  • Oral & Maxillofacial Surgery (AREA)
  • Molecular Biology (AREA)
  • Biomedical Technology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Epidemiology (AREA)
  • Robotics (AREA)
  • Dentistry (AREA)
  • Pathology (AREA)
  • Primary Health Care (AREA)
  • Radiology & Medical Imaging (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Urology & Nephrology (AREA)
  • Human Computer Interaction (AREA)
  • Gynecology & Obstetrics (AREA)
  • Dental Tools And Instruments Or Auxiliary Dental Instruments (AREA)
  • Dental Prosthetics (AREA)
  • Manipulator (AREA)

Claims (10)

  1. Ein Dentalimplantationssystem (100), umfassend:
    eine Patienteninteraktionsvorrichtung (150), welches ein Instrument (500) aufweist, welches ausgebildet ist, mindestens mit einem Ort innerhalb des Mundes eines Patienten zu interagieren und diesen zur Aufnahme eines Dentalimplantats vorzubereiten;
    eine Führungsvorrichtung (200) in Verbindung mit einem Referenzmarker (250), welcher mit dem Mund des Patienten in Eingriff bringbar ist, wobei die Führungsvorrichtung (200) dazu ausgebildet ist, die Patienteninteraktionsvorrichtung (150) aufzunehmen und das Instrument (500) der Patienteninteraktionsvorrichtung (150) relativ zu dem Referenzmarker (250) in Verbindung mit einer Manipulation der Patienteninteraktionsvorrichtung (150) durch einen Benutzer zu führen;
    eine Kontrollvorrichtung (450), welche einen Prozessor umfasst, wobei die Kontrollvorrichtung (450) ausgebildet ist, mit der Führungsvorrichtung (200) in Verbindung zu stehen und die Patienteninteraktionsvorrichtung (150) über die Führungsvorrichtung (200) zu lenken, um den Ort vorzubereiten, um das Dentalimplantat aufzunehmen; und
    einen Eingriffssensor (750), welcher mit der Patienteninteraktionsvorrichtung (150) in Wirkeingriff steht und ausgebildet ist, mit der Kontrollvorrichtung (450) in Verbindung zu stehen, wobei der Eingriffssensor (750) ausgebildet ist, ein Außereingriffkommen zwischen der Patienteninteraktionsvorrichtung (150) und dem Benutzer zu erfassen und das Außereingriffkommen an die Kontrollvorrichtung (450) zu übermitteln, wobei die Kontrollvorrichtung (450) auf das erfasste Außereingriffkommen anspricht, um die Führungsvorrichtung (200) zu lenken, um die Patienteninteraktionsvorrichtung (150) mindestens bei einer minimalen vertikalen Anordnung aufrechtzuerhalten.
  2. Das System nach Anspruch 1, wobei die Kontrollvorrichtung (450):
    ferner dazu ausgebildet ist, auf das erfasste Außereingriffkommen zwischen der Patienteninteraktionsvorrichtung (150) und dem Benutzer anzusprechen, um die Führungsvorrichtung (200) zu lenken, um die Patienteninteraktionsvorrichtung (150) bei einem von einer lateralen Anordnung und einer rotatorischen Ausrichtung aufrechtzuerhalten;
    ferner dazu ausgebildet ist, auf ein Ineingriffkommen zwischen der Patienteninteraktionsvorrichtung (150) und dem Benutzer anzusprechen, um die Führungsvorrichtung (200) zu betätigen, um mindestens das Instrument der Patienteninteraktionsvorrichtung (150) relativ zu dem Referenzmarker (250) zu führen;
    ferner dazu ausgebildet ist, auf ein Ineingriffkommen zwischen der Patienteninteraktionsvorrichtung (150) und dem Benutzer anzusprechen, um mindestens eine Betätigung des Instruments (500) zu erlauben; oder
    ferner dazu ausgebildet ist, auf ein Ineingriffkommen zwischen der Patienteninteraktionsvorrichtung (150) und dem Benutzer anzusprechen, um einen virtuellen Implantationsplan zum Führen mindestens des Instruments (500) der Patienteninteraktionsvorrichtung (150) zu betätigen.
  3. Das System nach Anspruch 1, wobei der Eingriffssensor (750) eines von einem berührungsempfindlichen Aktuator, einem druckempfindlichen Aktuator, einem optischen Aktuator und einem akustischen Aktuator umfasst, welche mit der Patienteninteraktionsvorrichtung (150) assoziiert sind.
  4. Das System nach Anspruch 1 oder 2, wobei mindestens eines von dem Eingriffssensor (750) und dem Referenzmarker (250) dazu ausgebildet ist,
    mit der Kontrollvorrichtung (450) über eines von einem elektrischen Kommunikationssystem, einem mechanischen Kommunikationssystem, einem elektromechanischen Kommunikationssystem, einem optischen Kommunikationssystem und Kombinationen hiervon in Verbindung zu stehen; oder dazu ausgebildet ist,
    mit der Kontrollvorrichtung (450) über eines von einem drahtlosen Kommunikationssystem und einem drahtgebundenen Kommunikationssystem in Verbindung zu stehen.
  5. Das System nach einem der Ansprüche 1 bis 4, ferner umfassend mindestens einen Kraftsensor, welcher mit mindestens einem von der Führungsvorrichtung (200) und der Patienteninteraktionsvorrichtung (150) in Wirkeingriff steht, wobei der mindestens eine Kraftsensor dazu ausgebildet ist, eine auf die Patienteninteraktionsvorrichtung (150) wirkende Kraft zu messen und die gemessene Kraft an die Kontrollvorrichtung (450) zu übermitteln.
  6. Das System nach Anspruch 5, wobei die Kontrollvorrichtung (450) auf ein Außereingriffkommen von dem Eingriffssensor (750) durch den Benutzer anspricht, um die gemessene Kraft von dem mindestens einen Kraftsensor zu nullen.
  7. Das System nach einem der Ansprüche 1 bis 6, wobei die Kontrollvorrichtung (450) ausgebildet ist, einen virtuellen Implantationsplan für den Ort innerhalb des Mundes des Patienten auszuführen und die Führungsvorrichtung (200) gemäß dem virtuellen Implantationsplan zu lenken, als Antwort auf das Ineingriffkommen des Eingriffssensors (750) durch den Benutzer.
  8. Das System nach Anspruch 7, wobei die Kontrollvorrichtung (450)
    dazu ausgebildet ist, eine taktile Rückmeldung via Patienteninteraktionsvorrichtung (150) an den Benutzer zu richten, wenn das von dem Benutzer manipulierte Instrument (500) von dem virtuellen Implantationsplan abweicht; oder
    dazu ausgebildet ist, mindestens eines von einer Audio-Rückmeldung und einer visuellen Rückmeldung via mindestens eines von Kontrollvorrichtung (450) und Patienteninteraktionsvorrichtung (150) an den Benutzer zu richten, wenn das von dem Benutzer manipulierte Instrument (500) von dem virtuellen Implantationsplan abweicht.
  9. Das System nach einem der Ansprüche 1 bis 8, ferner umfassend eine Anzeigevorrichtung (800), welche ausgebildet ist, eine Echtzeitdarstellung von mindestens dem Instrument (500) der Patienteninteraktionsvorrichtung (150) in Bezug auf eine Darstellung des Mundes des Patienten während des Eingriffs mit der Patienteninteraktionsvorrichtung (150) und deren Manipulation durch den Benutzer anzuzeigen.
  10. Das System nach Anspruch 9, wobei die Kontrollvorrichtung (450) ausgebildet ist, mit der Führungsvorrichtung (200) und der Anzeigevorrichtung (800) in Verbindung zu stehen, und wobei die Kontrollvorrichtung (450) ausgebildet ist, eine Manipulation mindestens des Instruments (500) der Patienteninteraktionsvorrichtung (150) in Bezug auf den Mund des Patienten, welche mindestens teilweise über die Führungsvorrichtung (200) erfolgt, zu überwachen und eine damit assoziierte Information an die Anzeigevorrichtung (800) zu richten.
EP16705612.6A 2015-01-22 2016-01-21 Interaktive führungs- und manipulationsdetektionsanordnungen für ein chirurgisches robotersystem Active EP3247306B1 (de)

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EP19214977.1A Division-Into EP3653162B1 (de) 2015-01-22 2016-01-21 Interaktive führungs- und manipulationsdetektionsanordnungen für ein chirurgisches robotisches system und zugehöriges verfahren

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Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2552137A (en) * 2016-07-03 2018-01-17 Tarazi Eyal Systems and methods of automated control of in-situ preparation for prefabricated fixed dental prosthesis
EP3509470A4 (de) * 2016-09-11 2020-07-22 Perioendoscopy, LLC Gehäuseanordnung für periodontale endoskopsonde
US11259894B2 (en) * 2016-09-19 2022-03-01 Neocis, Inc. Tracking and guidance arrangement for a surgical robot system and related method
TWI783995B (zh) * 2017-04-28 2022-11-21 美商尼奧西斯股份有限公司 進行導引口腔顎面程序方法及相關系統
CN107595418A (zh) * 2017-09-15 2018-01-19 杭州术康医疗科技有限公司 一种自动种植牙科机器人
EP3735696A1 (de) * 2018-01-02 2020-11-11 Koninklijke Philips N.V. Animierte positionsanzeige einer oss-interventionsvorrichtung
CN108433834A (zh) * 2018-04-09 2018-08-24 上海术凯机器人有限公司 一种牙科种植钻针配准装置和方法
WO2019215512A1 (en) * 2018-05-10 2019-11-14 Cyberdontics Inc. Automated dental drill
CN113143353B (zh) * 2018-08-24 2023-03-17 上海微创医疗机器人（集团）股份有限公司 蛇形手术器械
US11612438B2 (en) * 2018-09-05 2023-03-28 Point Robotics Medtech Inc. Navigation system and method for medical operation by a robotic system using a tool
EP3725231B1 (de) * 2019-04-17 2021-07-21 Sirona Dental Systems GmbH Vorrichtung zur echtzeitvisualisierung einer bewegung eines unterkiefers gegenüber einem oberkiefer in einem kraniomaxillofazialen bereich eines patienten in der zahnärztlichen diagnostik
CN111227967A (zh) * 2020-03-24 2020-06-05 卡瓦科尔牙科医疗器械（苏州）有限公司 具有无线控制器的牙科种植机
KR102367635B1 (ko) * 2020-04-01 2022-02-28 주식회사 푸른기술 치과 임플란트 수술 보조용 로봇시스템
WO2021220041A1 (en) * 2020-05-01 2021-11-04 Khan Ahmadi Nikoo Smart jaw drilling machine in implant placement
TWI777902B (zh) * 2022-03-11 2022-09-11 柯百俞 植牙之工作角度導引裝置及其方法

Family Cites Families (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2808366B1 (fr) * 2000-04-26 2003-12-19 Univ Paris Vii Denis Diderot Procede et systeme d'apprentissage en realite virtuelle, et application en odontologie
EP1219260B1 (de) * 2000-12-19 2003-06-25 BrainLAB AG Verfahren und Vorrichtung zur navigationsgestüzten Zahnbehandlung
US8010180B2 (en) * 2002-03-06 2011-08-30 Mako Surgical Corp. Haptic guidance system and method
US20050116673A1 (en) * 2003-04-18 2005-06-02 Rensselaer Polytechnic Institute Methods and systems for controlling the operation of a tool
US7702139B2 (en) * 2006-10-13 2010-04-20 Carestream Health, Inc. Apparatus for caries detection
TWI396523B (zh) * 2007-02-14 2013-05-21 Been Der Yang 用以加速牙科診斷及手術規劃之系統及其方法
CA2713122A1 (en) * 2008-01-23 2009-07-30 Sensable Technologies, Inc. Haptically enabled dental modeling system
KR101557383B1 (ko) 2008-04-02 2015-10-05 네오시스, 엘엘씨 유도 치과용 임플란트 시스템, 관련 장치 및 임플란트 방법
KR101054072B1 (ko) * 2009-05-19 2011-08-03 박성백 임플란트 시술용 전동기기
WO2011091382A1 (en) * 2010-01-22 2011-07-28 Precision Through Imaging, Llc Dental implantation system and method
CA2805106C (en) * 2010-07-12 2016-04-05 9104-6516 Quebec Inc. Dental analysis method and system
US20120062557A1 (en) * 2010-09-10 2012-03-15 Dimensional Photonics International, Inc. Systems and methods for processing and displaying intra-oral measurement data
ES2776151T3 (es) * 2011-02-25 2020-07-29 Corin Ltd Un método implementado por ordenador para proporcionar datos de información de alineación para la alineación de un implante ortopédico para una articulación de un paciente
EP2693975B1 (de) * 2011-04-07 2018-11-28 3Shape A/S 3d-system zum führen von objekten
DE102011050192A1 (de) * 2011-05-06 2012-11-08 Aesculap Ag Chirurgisches Kupplungssystem und chirurgisches Antriebssystem
RU2745030C2 (ru) * 2011-05-26 2021-03-18 Вайэкс Дентал Текнолоджиз, Ллк Стоматологический инструмент и направляющие устройства
DE102011080180B4 (de) * 2011-08-01 2013-05-02 Sirona Dental Systems Gmbh Verfahren zur Registrierung mehrerer dreidimensionaler Aufnahmen eines dentalen Objektes
US9827076B2 (en) * 2011-12-22 2017-11-28 3M Innovative Properties Company Method and system for making a dental restoration
US20130261433A1 (en) * 2012-03-28 2013-10-03 Navident Technologies, Inc. Haptic simulation and surgical location monitoring system and method
US9198627B2 (en) * 2012-04-16 2015-12-01 Biomet 3i System and method for improved intra-oral scanning protocol and calibration
JP2013236749A (ja) * 2012-05-15 2013-11-28 Denso Corp 歯科インプラント手術支援装置
CN111485226A (zh) * 2012-07-27 2020-08-04 应用材料公司 粗糙化的基板支撑件
US20140178832A1 (en) * 2012-12-21 2014-06-26 Anatomage Inc. System and method for providing compact navigation-based surgical guide in dental implant surgery
US9468504B2 (en) * 2013-02-27 2016-10-18 B & D Dental Corporation Dental cutting system and method with remote cutting guide
US9877810B2 (en) * 2013-03-15 2018-01-30 Neocis Inc. Method for conducting a guided sinus lift procedure
US9962234B2 (en) * 2014-12-24 2018-05-08 Isethco Llc Disposable surgical intervention guides, methods, and kits

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
None *

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ES2797683T3 (es) 2020-12-03
CN107405180B (zh) 2020-03-24
IL273356A (en) 2020-05-31
IL253594A0 (en) 2017-09-28
IL253594B (en) 2020-04-30
CN107405180A (zh) 2017-11-28
EP3653162A1 (de) 2020-05-20
IL273356B (en) 2022-10-01
EP3653162B1 (de) 2023-07-19
US20170319302A1 (en) 2017-11-09
EP3247306A1 (de) 2017-11-29
WO2016118737A1 (en) 2016-07-28
KR20170110632A (ko) 2017-10-11
KR102005751B1 (ko) 2019-07-31
US11033366B2 (en) 2021-06-15
IL273356B2 (en) 2023-02-01
ES2960538T3 (es) 2024-03-05

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